Literature DB >> 32500617

Selective recovery of ammonia nitrogen from wastewaters with transition metal-loaded polymeric cation exchange adsorbents.

Brandon Clark1, William Tarpeh2.   

Abstract

Extracting valuable products from wastewaters with nitrogen-selective adsorbents can offset energy-intensive ammonia production, rebalance the nitrogen cycle, and incentivize environmental remediation. Separating nitrogen (N) as ammonium from other wastewater cations (e.g., K + , Ca 2+ ) presents a major challenge to N removal from wastewater and N recovery as high-purity products. We achieved high selectivity and capacity via ligand exchange of ammonia with ammine-complexing transition metals loaded onto polymeric cation exchange resins. Compared to commercial resins, metal-ligand exchange adsorbents exhibited higher ammonia removal capacity (8 meq/g) and selectivity (N/K + equilibrium selectivity of 10.1) in binary equimolar solutions. Considering optimal ammonia concentrations (200-300 meq/L) and pH (9-10) for metal-ligand exchange, we identified hydrolyzed urine as a promising candidate for selective TAN recovery. However, divalent cation exchange increased transition metal elution and reduced ammonia adsorption. Ultimately, metal-ligand exchange adsorbents can advance nitrogen-selective separations from wastewaters.
© 2020 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  Ion exchange; Ligand design; Resource recovery; Waste prevention; Water chemistry

Year:  2020        PMID: 32500617     DOI: 10.1002/chem.202002170

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  2 in total

1.  The urine revolution: how recycling pee could help to save the world.

Authors:  Chelsea Wald
Journal:  Nature       Date:  2022-02       Impact factor: 49.962

Review 2.  Making wastewater obsolete: Selective separations to enable circular water treatment.

Authors:  William A Tarpeh; Xi Chen
Journal:  Environ Sci Ecotechnol       Date:  2021-01-06
  2 in total

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